no MONDO ID for mitochondrial_dna_depletion_syndrome_14 -> OPA1 (SPBC1718.06)
no MONDO ID for behr_syndrome -> OPA1 (SPBC1718.06)
no MONDO ID for optic_atrophy_with_or_without_deafness_ophthalmoplegia_myopathy_ataxia_and_neuropathy -> OPA1 (SPBC1718.06)
MONDO:0014253 is obsolete (consider: MONDO:8000024) - skipping annotation for SPAC17G8.14c,SPBC12D12.04c / autoimmune_lymphoproliferative_syndrome_type_iii
MONDO:0020734 is obsolete (no "replaced_by" or "consider" tag) - skipping annotation for SPBC106.04 / erythrocyte_amp_deaminase_deficiency
no MONDO ID for glaucoma_normal_tension -> OPA1 (SPBC1718.06)
no MONDO ID for autosomal_dominant_optic_atrophy_plus_syndrome -> OPA1 (SPBC1718.06)
ValWood
commented
2 years ago
no MONDO ID for mitochondrial_dna_depletion_syndrome_14 -> OPA1 (SPBC1718.06) no MONDO ID for behr_syndrome -> OPA1 (SPBC1718.06) no MONDO ID for optic_atrophy_with_or_without_deafness_ophthalmoplegia_myopathy_ataxia_and_neuropathy -> OPA1 (SPBC1718.06) MONDO:0014253 is obsolete (consider: MONDO:8000024) - skipping annotation for SPAC17G8.14c,SPBC12D12.04c / autoimmune_lymphoproliferative_syndrome_type_iii MONDO:0020734 is obsolete (no "replaced_by" or "consider" tag) - skipping annotation for SPBC106.04 / erythrocyte_amp_deaminase_deficiency no MONDO ID for glaucoma_normal_tension -> OPA1 (SPBC1718.06) no MONDO ID for autosomal_dominant_optic_atrophy_plus_syndrome -> OPA1 (SPBC1718.06)